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Luteoforol

From Wikipedia, the free encyclopedia
Luteoforol
Chemical structure of luteoforol
Chemical structure of luteoforol
Names
IUPAC name
(2S)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-4,5,7-triol
Other names
3-Deoxyleucocyanidin
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
UNII
  • InChI=1S/C15H14O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,12-13,16-20H,6H2/t12?,13-/m0/s1
    Key: FSYDWKPCKNCRDI-ABLWVSNPSA-N
  • C1C(C2=C(C=C(C=C2OC1C3=CC(=C(C=C3)O)O)O)O)O
Properties
C15H14O6
Molar mass290.26 g/mol
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound

Luteoforol is a chemical compound belonging to theflavan-4-ol class of flavonoids.

Luteoforol is induced inpome fruits byprohexadione-calcium.[1]

References

[edit]
  1. ^Spinelli, Francesco; Speakman, John-Bryan; Rademacher, Wilhelm; Halbwirth, Heidi; Stich, Karl; Costa, Guglielmo (2005)."Luteoforol, a flavan 4-ol, is induced in pome fruits by prohexadione-calciumand shows phytoalexin-like properties against Erwinia amylovora and other plant pathogens".European Journal of Plant Pathology.112 (2):133–142.doi:10.1007/s10658-005-2192-x.S2CID 897040.
Types offlavan-4-ols
Flavan-4-ols:
Glycosides
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